Freyr Provides End-to-end Medical device regulatory consulting support for medical devices and IVD companies that span across device registration, classification, and market access of products in compliance with Country-specific regulations across globe.

Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.

Freyr provides Swiss Authorized Representative (CH-REP) services to foreign medical device manufacturers for their product registration and market entry in Switzerland and acts as single point of contact in the Country for liaison with Regulatory Agency.

Freyr provides regulatory services and solutions in Thailand to comply with Thailand FDA for pharma, medical device, cosmetics, and food supplement manufacturer companies.